ClearanceBrief
Company ยท US

Celonova Biosciences, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2008 to 2014. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KRDDevice, Vascular, For Promoting Embolization4
NAJAgents, Embolic, For Treatment Of Uterine Fibroids1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 7, 2014K141209EMBOZENE COLOR-ADVANCED MICROSPHERES, EMBOZENE OPAQUE (NON-COLORED) MICROSPHERES, ONCOZENE MICROSPHERES
Celonova Biosciences, Inc.
KRD
Feb 24, 2014K133447EMBOZENE COLOR-ADVANCED MICROSPHERES, EMBOZENE OPAQUE (NON-COLORED) MICROSPHERES
Celonova Biosciences, Inc.
NAJ
Oct 3, 2013K132675EMBOZENE MICROSPHERES
Celonova Biosciences, Inc.
KRD
Mar 4, 2013K130307ONCOZENE MICROSPHERES 40UM, 2ML, ONCOZENE MICROSPHERES 75UM, 2ML, ONCOZENE MICROSPHERES 100UM, 2ML, ONCOZENE MICROSPHERE
Celonova Biosciences, Inc.
KRD
Dec 15, 2008K073417EMBOZENE MICROSPHERES
Celonova Biosciences, Inc.
KRD

Latest recalls

DateFirm and productCodeLinked 510(k)
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